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Alopecia Areata Universalis in the Onset of Autoimmune Polyendocrine Syndrome Type III C

Alopecia areata (AA) is an organ-specific autoimmune disease which affects hair follicles. It usually presents as a transient patchy hair loss, but it can sometimes progress into more severe forms such as AA totalis or AA universalis (AAU). Different autoimmune diseases, as well as autoimmune polygl...

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Detalles Bibliográficos
Autores principales: Neagu, Nicoleta, Morariu, Silviu Horia, Grama, Alina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069905/
https://www.ncbi.nlm.nih.gov/pubmed/35531483
http://dx.doi.org/10.4103/ijt.ijt_77_20
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author Neagu, Nicoleta
Morariu, Silviu Horia
Grama, Alina
author_facet Neagu, Nicoleta
Morariu, Silviu Horia
Grama, Alina
author_sort Neagu, Nicoleta
collection PubMed
description Alopecia areata (AA) is an organ-specific autoimmune disease which affects hair follicles. It usually presents as a transient patchy hair loss, but it can sometimes progress into more severe forms such as AA totalis or AA universalis (AAU). Different autoimmune diseases, as well as autoimmune polyglandular syndromes (APS), have been associated with AA, especially with Type I and Type II APS. Herein, we describe the case of a 16-year-old boy with a severe form of AAU and early onset of adult APS, Type III C. As far as we are aware, this combination of AAU, Hashimoto thyroiditis, and Type I diabetes in a teenager has not been previously described in the literature. Furthermore, the early onset of AAU followed by a premature debut of adult APS Type III is again unique, which is why we report this case.
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spelling pubmed-90699052022-05-05 Alopecia Areata Universalis in the Onset of Autoimmune Polyendocrine Syndrome Type III C Neagu, Nicoleta Morariu, Silviu Horia Grama, Alina Int J Trichology Case Report Alopecia areata (AA) is an organ-specific autoimmune disease which affects hair follicles. It usually presents as a transient patchy hair loss, but it can sometimes progress into more severe forms such as AA totalis or AA universalis (AAU). Different autoimmune diseases, as well as autoimmune polyglandular syndromes (APS), have been associated with AA, especially with Type I and Type II APS. Herein, we describe the case of a 16-year-old boy with a severe form of AAU and early onset of adult APS, Type III C. As far as we are aware, this combination of AAU, Hashimoto thyroiditis, and Type I diabetes in a teenager has not been previously described in the literature. Furthermore, the early onset of AAU followed by a premature debut of adult APS Type III is again unique, which is why we report this case. Wolters Kluwer - Medknow 2022 2022-04-04 /pmc/articles/PMC9069905/ /pubmed/35531483 http://dx.doi.org/10.4103/ijt.ijt_77_20 Text en Copyright: © 2022 International Journal of Trichology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Neagu, Nicoleta
Morariu, Silviu Horia
Grama, Alina
Alopecia Areata Universalis in the Onset of Autoimmune Polyendocrine Syndrome Type III C
title Alopecia Areata Universalis in the Onset of Autoimmune Polyendocrine Syndrome Type III C
title_full Alopecia Areata Universalis in the Onset of Autoimmune Polyendocrine Syndrome Type III C
title_fullStr Alopecia Areata Universalis in the Onset of Autoimmune Polyendocrine Syndrome Type III C
title_full_unstemmed Alopecia Areata Universalis in the Onset of Autoimmune Polyendocrine Syndrome Type III C
title_short Alopecia Areata Universalis in the Onset of Autoimmune Polyendocrine Syndrome Type III C
title_sort alopecia areata universalis in the onset of autoimmune polyendocrine syndrome type iii c
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069905/
https://www.ncbi.nlm.nih.gov/pubmed/35531483
http://dx.doi.org/10.4103/ijt.ijt_77_20
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